The following data is part of a premarket notification filed by Site Microsurgical Systems, Inc. with the FDA for Iolab Power I.v. Pole.
Device ID | K921135 |
510k Number | K921135 |
Device Name: | IOLAB POWER I.V. POLE |
Classification | Unit, Phacofragmentation |
Applicant | SITE MICROSURGICAL SYSTEMS, INC. 135 GIBRALTAR RD. Horsham, PA 19044 |
Contact | James K Mccracken |
Correspondent | James K Mccracken SITE MICROSURGICAL SYSTEMS, INC. 135 GIBRALTAR RD. Horsham, PA 19044 |
Product Code | HQC |
CFR Regulation Number | 886.4670 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-03-10 |
Decision Date | 1992-06-03 |